770785002: T-cell immunodeficiency due to ras homolog family member H deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\T-cell immunodeficiency due to ras homolog family member H deficiency
• \Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\T-cell immunodeficiency due to ras homolog family member H deficiency

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3702782013	T-cell immunodeficiency due to RHOH (ras homolog family member H) deficiency	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3702783015	T-cell immunodeficiency with epidermodysplasia verruciformis	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3702784014	T-cell immunodeficiency due to RHOH deficiency	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3702786011	T-cell immunodeficiency due to ras homolog family member H deficiency	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3702787019	T-cell immunodeficiency due to ras homolog family member H deficiency (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

Back to Start